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Found 15 results
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Lunetta, Kathryn L
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2021
Kunkle BW
,
Schmidt M
,
Klein H-U
,
Naj AC
,
Hamilton-Nelson KL
,
Larson EB
,
Evans DA
,
De Jager PL
,
Crane PK
,
Buxbaum JD
et al.
. 2021.
Novel Alzheimer Disease Risk Loci and Pathways in African American Individuals Using the African Genome Resources Panel: A Meta-analysis.
.
JAMA Neurol. 78(1):102-113.
2019
Patel D
,
Mez J
,
Vardarajan BN
,
Staley L
,
Chung J
,
Zhang X
,
Farrell JJ
,
Rynkiewicz MJ
,
Cannon-Albright LA
,
Teerlink CC
et al.
. 2019.
Association of Rare Coding Mutations With Alzheimer Disease and Other Dementias Among Adults of European Ancestry.
.
JAMA Netw Open. 2(3):e191350.
2018
Blue EE
,
Bis JC
,
Dorschner MO
,
Tsuang DW
,
Barral SM
,
Beecham G
,
Below JE
,
Bush WS
,
Butkiewicz M
,
Cruchaga C
et al.
. 2018.
Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project.
.
Dement Geriatr Cogn Disord. 45(1-2):1-17.
Ikezu T
,
Chen CD
,
DeLeo AM
,
Zeldich E
,
M Fallin D
,
Kanaan NM
,
Lunetta KL
,
Abraham CR
,
Logue MW
,
Farrer LA
. 2018.
Tau Phosphorylation is Impacted by Rare AKAP9 Mutations Associated with Alzheimer Disease in African Americans.
.
J Neuroimmune Pharmacol. 13(2):254-264.
2017
Mez J
,
Chung J
,
Jun G
,
Kriegel J
,
Bourlas AP
,
Sherva R
,
Logue MW
,
Barnes LL
,
Bennett DA
,
Buxbaum JD
et al.
. 2017.
Two novel loci, COBL and SLC10A2, for Alzheimer's disease in African Americans.
.
Alzheimers Dement. 13(2):119-129.
2016
Hohman TJ
,
Cooke-Bailey JN
,
Reitz C
,
Jun G
,
Naj A
,
Beecham GW
,
Liu Z
,
Carney RM
,
Vance JM
,
Cuccaro ML
et al.
. 2016.
Global and local ancestry in African-Americans: Implications for Alzheimer's disease risk.
.
Alzheimers Dement. 12(3):233-43.
2015
Ghani M
,
Reitz C
,
Cheng R
,
Vardarajan BNarayan
,
Jun G
,
Sato C
,
Naj A
,
Rajbhandary R
,
Wang L-S
,
Valladares O
et al.
. 2015.
Association of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals.
.
JAMA Neurol. 72(11):1313-23.
Nho K
,
Kim S
,
Risacher SL
,
Shen L
,
Corneveaux JJ
,
Swaminathan S
,
Lin H
,
Ramanan VK
,
Liu Y
,
Foroud TM
et al.
. 2015.
Protective variant for hippocampal atrophy identified by whole exome sequencing.
.
Ann Neurol. 77(3):547-52.
Wang L-S
,
Naj AC
,
Graham RR
,
Crane PK
,
Kunkle BW
,
Cruchaga C
,
Murcia JDGonzalez
,
Cannon-Albright L
,
Baldwin CT
,
Zetterberg H
et al.
. 2015.
Rarity of the Alzheimer disease-protective APP A673T variant in the United States.
.
JAMA Neurol. 72(2):209-16.
2014
Naj AC
,
Jun G
,
Reitz C
,
Kunkle BW
,
Perry W
,
Park YSon
,
Beecham GW
,
Rajbhandary RA
,
Hamilton-Nelson KL
,
Wang L-S
et al.
. 2014.
Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study.
.
JAMA Neurol. 71(11):1394-404.
Jun G
,
Asai H
,
Zeldich E
,
Drapeau E
,
Chen CD
,
Chung J
,
Park J-H
,
Kim S
,
Haroutunian V
,
Foroud T
et al.
. 2014.
PLXNA4 is associated with Alzheimer disease and modulates tau phosphorylation.
.
Ann Neurol. 76(3):379-92.
2013
Reitz C
,
Jun G
,
Naj A
,
Rajbhandary R
,
Vardarajan BNarayan
,
Wang L-S
,
Valladares O
,
Lin C-F
,
Larson EB
,
Graff-Radford NR
et al.
. 2013.
Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ϵ4,and the risk of late-onset Alzheimer disease in African Americans.
.
JAMA. 309(14):1483-92.
2012
Jun G
,
Vardarajan BN
,
Buros J
,
Yu C-E
,
Hawk MV
,
Dombroski BA
,
Crane PK
,
Larson EB
,
Mayeux R
,
Haines JL
et al.
. 2012.
Comprehensive search for Alzheimer disease susceptibility loci in the APOE region.
.
Arch Neurol. 69(10):1270-9.
2011
Naj AC
,
Jun G
,
Beecham GW
,
Wang L-S
,
Vardarajan BNarayan
,
Buros J
,
Gallins PJ
,
Buxbaum JD
,
Jarvik GP
,
Crane PK
et al.
. 2011.
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.
.
Nat Genet. 43(5):436-41.
2010
Jun G
,
Naj AC
,
Beecham GW
,
Wang L-S
,
Buros J
,
Gallins PJ
,
Buxbaum JD
,
Ertekin-Taner N
,
M Fallin D
,
Friedland R
et al.
. 2010.
Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes.
.
Arch Neurol. 67(12):1473-84.